Canonical Allele Identifier: CA366234671

Gene: ARID1B

Linked Data

• dbSNP Id: rs1489287750
• gnomAD v2: 6-157511180-C-T
• gnomAD v4: 6-157190046-C-T
• MyVariant Identifiers: chr6:g.157511180C>T (hg19) ; chr6:g.157190046C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190046C>T , CM000668.2:g.157190046C>T	GRCh38
NC_000006.11:g.157511180C>T , CM000668.1:g.157511180C>T	GRCh37
NC_000006.10:g.157552872C>T	NCBI36
NG_032093.1:g.417117C>T
NG_032093.2:g.417117C>T
NG_066624.1:g.419021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3908C>T	ENSP00000055163.8:p.Thr1303Ile
ENST00000414678.8:c.3977C>T	ENSP00000412835.3:p.Thr1326Ile
ENST00000637015.2:c.4196C>T	ENSP00000489729.2:p.Thr1399Ile
ENST00000346085.10:c.3947C>T	ENSP00000344546.5:p.Thr1316Ile
ENST00000350026.10:c.3659C>T	ENSP00000055163.7:p.Thr1220Ile
ENST00000414678.7:c.2225C>T	ENSP00000412835.2:p.Thr742Ile
ENST00000635849.1:c.1388C>T	ENSP00000490948.1:p.Thr463Ile
ENST00000635957.1:c.1019C>T	ENSP00000490385.1:p.Thr340Ile
ENST00000636930.2:c.4067C>T MANE Select	ENSP00000490491.2:p.Thr1356Ile
ENST00000636940.1:n.2064C>T
ENST00000637015.1:c.1435C>T
ENST00000637568.1:c.1349C>T
ENST00000637741.1:n.733C>T
ENST00000637810.1:c.1409C>T	ENSP00000489636.1:p.Thr470Ile
ENST00000637904.1:c.1568C>T	ENSP00000490550.1:p.Thr523Ile
ENST00000647938.1:c.3698C>T	ENSP00000498155.1:p.Thr1233Ile
ENST00000346085.9:c.3698C>T	ENSP00000344546.4:p.Thr1233Ile
ENST00000350026.9:c.3659C>T	ENSP00000055163.7:p.Thr1220Ile
ENST00000414678.6:c.2225C>T	ENSP00000412835.2:p.Thr742Ile
NM_017519.2:c.3659C>T	NP_059989.2:p.Thr1220Ile
NM_020732.3:c.3698C>T	NP_065783.3:p.Thr1233Ile
XM_005267069.3:c.3818C>T	XP_005267126.2:p.Thr1273Ile
XM_011535984.1:c.2897C>T	XP_011534286.1:p.Thr966Ile
XM_011535985.1:c.2717C>T	XP_011534287.1:p.Thr906Ile
XM_011535986.1:c.2477C>T	XP_011534288.1:p.Thr826Ile
XM_011535987.1:c.2096C>T	XP_011534289.1:p.Thr699Ile
XM_011535988.1:c.959C>T	XP_011534290.1:p.Thr320Ile
NM_001346813.1:c.3818C>T	NP_001333742.1:p.Thr1273Ile
NM_001363725.1:c.1568C>T	NP_001350654.1:p.Thr523Ile
XM_011535984.2:c.4028C>T	XP_011534286.2:p.Thr1343Ile
XM_011535988.3:c.959C>T	XP_011534290.1:p.Thr320Ile
XM_017011103.2:c.3929C>T	XP_016866592.1:p.Thr1310Ile
XM_017011104.1:c.3899C>T	XP_016866593.1:p.Thr1300Ile
XM_017011105.2:c.3869C>T	XP_016866594.1:p.Thr1290Ile
XM_017011106.2:c.3740C>T	XP_016866595.1:p.Thr1247Ile
XM_017011107.2:c.3719C>T	XP_016866596.1:p.Thr1240Ile
XR_002956289.1:n.4111C>T
NM_001363725.2:c.1568C>T	NP_001350654.1:p.Thr523Ile
NM_001371656.1:c.3947C>T	NP_001358585.1:p.Thr1316Ile
NM_001374820.1:c.3947C>T	NP_001361749.1:p.Thr1316Ile
NM_001374828.1:c.4067C>T MANE Select	NP_001361757.1:p.Thr1356Ile
NM_017519.3:c.3908C>T	NP_059989.3:p.Thr1303Ile